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  • Guest Post: Maia's CVID story
    Common Variable Immunodeficiency

    Guest Post: Maia’s CVID Story

    March 12, 2025 / 0 Comments
    read more
    Maia Marks

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    Are Plasma Treatments Painful?

    October 27, 2022
    world PI week 2024

    World PI Week 2024: Spreading Awareness For Primary Immunodeficiency

    April 17, 2024

    SCIg Series: Navigating anxiety about infusions

    May 13, 2023
  • rare disease day 20235 navigating life with common variable immunodeficiency for 6 years
    Common Variable Immunodeficiency

    Rare Disease Day 2025: Navigating life with Common Variable Immunodeficiency for 6 years

    February 26, 2025 / 0 Comments
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    Aubrey

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    What is immunoglobulin replacement therapy (Ig)?: My experience with starting Ig

    November 6, 2023
    What are immunoglobulins?

    What are immunoglobulins? How they relate to CVID

    July 2, 2023

    What are the Symptoms of Common Variable Immunodeficiency (CVID)?

    November 18, 2022
  • Finding hope after an upsetting diagnosis
    Chronic Illness

    Finding hope after an upsetting diagnosis

    June 7, 2024 / 0 Comments
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    Aubrey

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    When Chronic Illness is a Full Time Job

    November 30, 2022
    Life with primary immunodeficiency: How to stop yourself from spiraling when you feel symptoms coming on

    Life with primary immunodeficiency: How to stop yourself from spiraling when you feel symptoms coming on

    December 22, 2023
    How finding hobbies has improved my mental health as a young adult with chronic illness

    How finding hobbies improved my mental health as a young adult with chronic illness

    January 3, 2024
  • world PI week 2024
    Common Variable Immunodeficiency

    World PI Week 2024: Spreading Awareness For Primary Immunodeficiency

    April 17, 2024 / 0 Comments
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    Aubrey

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    Living with CVID: How chronic illness changed my outlook on life.

    April 11, 2023
    SCIG

    SCIg Series: sometimes I really don’t want to do it.

    March 31, 2023
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    National Primary Immunodeficiency Month: 3 Ways to Celebrate Your Strength

    April 25, 2023
  • telling your chronic illness story, an intimidating yet rewarding experience
    Chronic Illness

    Telling your chronic illness story: An intimidating yet rewarding experience

    March 15, 2024 / 0 Comments
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    Aubrey

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    Chronic Illness and Health Insurance

    Chronic Illness and Health Insurance: An eye opening experience

    July 20, 2023
    Life with chronic illness how to feel confident in your own skin

    Life with chronic illness: How to feel confident in your own skin

    November 1, 2023
    real talk real women podcast

    Listen to my guest feature: Real Talk Real Women by Gemma Serenity Gorokhoff

    June 20, 2023
  • A little health update: Dealing with mysterious low white blood cell counts
    Chronic Illness

    A little health update: Dealing with mysterious low white blood cell counts

    February 26, 2024 / 1 Comment
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    Aubrey

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    When Chronic Illness is a Full Time Job

    November 30, 2022
    Mixed feelings about life with chronic illness: It's okay to be happy and sad at the same time

    Mixed feelings about life with chronic illness: It’s okay to be happy and sad at the same time

    September 13, 2024
    the importance of hydration

    The importance of hydration for those with chronic illness (and everyone!)

    July 11, 2023
  • Life with primary immunodeficiency: How to stop yourself from spiraling when you feel symptoms coming on
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    Life with primary immunodeficiency: How to stop yourself from spiraling when you feel symptoms coming on

    December 22, 2023 / 0 Comments
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    Aubrey

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    Rare Disease Day 2023: raising awareness for over 6,000 rare diseases

    March 1, 2023
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    What is Primary Immunodeficiency? 3 things I’ve learned about PI

    March 24, 2023
    Mixed feelings about life with chronic illness: It's okay to be happy and sad at the same time

    Mixed feelings about life with chronic illness: It’s okay to be happy and sad at the same time

    September 13, 2024
  • what is immunoglobulin replacement therapy
    Common Variable Immunodeficiency

    What is immunoglobulin replacement therapy (Ig)?: My experience with starting Ig

    November 6, 2023 / 1 Comment
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    Aubrey

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    SCIg Series: Navigating anxiety about infusions

    May 13, 2023

    “Invisible” – a short film by me!

    August 1, 2022
    Reflecting on four years with common variable immunodeficiency CVID

    Reflecting on four years with Common Variable Immunodeficiency (CVID)

    August 23, 2023
  • what is an invisible illness?
    Chronic Illness

    What is an invisible illness? Navigating conditions that can’t be seen

    October 10, 2023 / 1 Comment
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    Aubrey

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    Telling People About Your Chronic Illness: 3 Ways to Feel Seen and Known

    January 19, 2023

    Creating a Sanctuary

    August 6, 2022
    Chronic Illness and Health Insurance

    Chronic Illness and Health Insurance: An eye opening experience

    July 20, 2023
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    Common Variable Immunodeficiency

    IDF’s Walk for Primary Immunodeficiency – how to get involved!

    September 11, 2023 / 2 Comments
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    Aubrey

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    CVID Symptoms: How do I live a “normal” life?

    March 21, 2023
    Guest Post: Maia's CVID story

    Guest Post: Maia’s CVID Story

    March 12, 2025
    rare disease day 20235 navigating life with common variable immunodeficiency for 6 years

    Rare Disease Day 2025: Navigating life with Common Variable Immunodeficiency for 6 years

    February 26, 2025
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About Me

I'm Aubrey, a young adult living with CVID in sunny San Diego!
Read more about me here!

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